EP0277222A4 - Modifizierte succinimide. - Google Patents

Modifizierte succinimide.

Info

Publication number
EP0277222A4
EP0277222A4 EP19870905836 EP87905836A EP0277222A4 EP 0277222 A4 EP0277222 A4 EP 0277222A4 EP 19870905836 EP19870905836 EP 19870905836 EP 87905836 A EP87905836 A EP 87905836A EP 0277222 A4 EP0277222 A4 EP 0277222A4
Authority
EP
European Patent Office
Prior art keywords
alkenyl
alkyl
group
succinimide
reaction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP19870905836
Other languages
English (en)
French (fr)
Other versions
EP0277222A1 (de
EP0277222B1 (de
Inventor
Robert H Wollenberg
Frank Plavac
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chevron USA Inc
Original Assignee
Chevron Research and Technology Co
Chevron Research Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chevron Research and Technology Co, Chevron Research Co filed Critical Chevron Research and Technology Co
Publication of EP0277222A1 publication Critical patent/EP0277222A1/de
Publication of EP0277222A4 publication Critical patent/EP0277222A4/de
Application granted granted Critical
Publication of EP0277222B1 publication Critical patent/EP0277222B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36—Oxygen or sulfur atoms
    • C07D207/40—2,5-Pyrrolidine-diones
    • C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
    • C07D207/408—Radicals containing only hydrogen and carbon atoms attached to ring carbon atoms
    • C07D207/412—Acyclic radicals containing more than six carbon atoms
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    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
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    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/224—Amides; Imides carboxylic acid amides, imides
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/234—Macromolecular compounds
    • C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
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    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/16—Amides; Imides
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    • C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
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    • C10M2207/02—Hydroxy compounds
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    • C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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    • C10M2215/086—Imides
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    • C10M2215/221—Six-membered rings containing nitrogen and carbon only
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    • C10M2215/223—Five-membered rings containing nitrogen and carbon only
    • C10M2215/224—Imidazoles
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    • C10M2215/30—Heterocyclic compounds
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    • C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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    • C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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    • C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04—Phosphate esters
    • C10M2223/045—Metal containing thio derivatives
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    • C10M2227/06—Organic compounds derived from inorganic acids or metal salts
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Definitions

  • This invention relates to additives which are useful as dispersants and/or detergents in lubricating oils.
  • this invention is directed toward polyamino alkenyl or alkyl succinimides wherein one or more of the amino nitrogens of the succinimide has been converted to a hydrocarbyl carbamate, a hydroxyhydrocar- bylcarbamate or a hydroxy polyoxyalkylene carbamate.
  • the modified polyamino alkenyl or alkyl succinimides of this invention have been found to possess improved dispersancy and/or detergency properties when employed in a lubricating oil.
  • These modified succinimides are also useful as detergents and/or dispersants in fuels.
  • Karol et al, U.S. Patent No. 4,460,381 discloses oxalic acid derivatives of mono-or bis-succinimides as fuel stabilizers.
  • Karol et al, U.S. Patent No. 4,482,464 discloses succinimides which have been modified by treatment with a hydroxyalkylene carboxylic acid selected from glycolic acid, lactic acid, 2-hydroxymethyl propionic acid and 2,2'-bis-hydroxy- methylpropionic acid. These modified succinimides of U.S. 4,482,464 are disclosed as lubricating oil additives.
  • U.S. 4,490,154 discloses fuels containing an alkenylsuccinyl polyglycolcarbonate ester as a deposit control additive.
  • U.S. 'Patent No. 3,216,936 discloses a product prepared from an aliphatic amine, a polymer substituted succinic acid and an aliphatic monocarboxylic acid. However, there is no teaching in these patents, or apparently elsewhere, to modify these polyamino alkenyl or alkyl succinimides in the manner of this invention.
  • polyamino alkenyl or alkyl succinimides may be modified to yield a polyamino alkenyl or alkyl succinimide wherein one or more of the nitrogens of the polyamino moiety is substituted with a hydrocarbyl oxycarbonyl, a hydroxyhydrocarbyl oxycarbonyl or a hydroxy poly(oxyalkylene) oxycarbonyl.
  • These modified succinimides are improved dispersants and/or detergents for use in fuels or oils. .
  • the instant invention is directed toward a multiply adducted alkenyl or alkyl succinimide wherein one or more of the nitrogens of the multiply adducted alkenyl or alkyl succinimide is substituted with a hydroxyhydrocarbyl oxycarbonyl wherein the hydroxyhydrocarbyl group of said hydroxyhydrocarbyl oxycarbonyl contains from 2 to 20 carbon atoms and 1 to 6 hydroxy groups with the proviso that there is no hydroxy substitution on the hydrocarbyl carbon atom attaching the hydroxyhydrocarbyl group to the oxy atom of the oxycarbonyl group and with the further proviso that when more than one hydroxy group is contained in the hydroxyhydrocarbyl group, no more than one hydroxy group is attached to the same carbon atom and the number of carbon atoms in the hydroxyhydrocarbyl group is minimally one greater than the number of hydroxy groups and wherein said multiply adducted alkenyl or alkyl succinimide wherein
  • the instant invention is directed toward a multiply adducted alkenyl or alkyl succinimide wherein one or more of the nitrogens of the multiply adducted alkenyl or alkyl succinimide is substituted with hydrocarbyl oxycarbonyl and wherein said multiply adducted alkenyl or alkyl succinimide is derived from a multiply adducted alkenyl or alkyl succinic anhydride characterized by the presence within its structure of an average of greater than 1 succinic group for each equivalent of alkenyl or alkyl group.
  • the instant invention is directed toward a multiply adducted alkenyl or alkyl succinimide wherein one or more of the nitrogens of the multiply adducted alkenyl or alkyl succinimide is substituted with a hydroxy poly(oxyalkylene) oxycarbonyl and wherein said multiply adducted alkenyl or alkyl succinimide is derived from a multiply adducted alkenyl or alkyl succinic anhydride characterized by the presence within its structure of an average of greater than 1 succinic group for each equivalent of alkenyl or alkyl group.
  • the instant invention is directed toward a product prepared by the process which comprises reacting at a temperature sufficient to cause reaction a multiply adducted alkenyl or alkyl succinimide containing at least one primary or secondary amine with a cyclic carbonate and wherein said multiply adducted alkenyl or alkyl succinimide is derived from a multiply adducted alkenyl or alkyl succinic anhydride characterized by the presence within its structure of an average of greater than 1 succinic group for each equivalent of alkenyl or alkyl group and wherein the molar change of the cyclic carbonate to the basic nitrogen of the multiply adducted alkenyl or alkyl succinimide is from about 0.2:1 to about 10:1.
  • a further aspect of this invention is a product prepared by the process which comprises contacting a multiply adducted alkenyl or alkyl succinimide with a polycarbonate at a temperature sufficient to cause reaction wherein the molar ratios of the individual carbonate units of said linear polycarbonate to the basic amine nitrogens of the multiply adducted alkenyl or alkyl succinimide is from about 0.1:1 to about 5:1 and wherein said multiply adducted alkenyl or alkyl succinimide is derived from a multiply adducted alkenyl or alkyl succinic anhydride characterized by the presence within its structure of greater than 1 succinic group for each equivalent of alkenyl or alkyl group.
  • the present invention also relates to a lubricating oil composition
  • a lubricating oil composition comprising a major amount of an oil of lubricating viscosity and an amount of a modified polyamino alkenyl or alkyl succinimide of this invention sufficient to provide dispersancy and/or detergency.
  • composition aspect of this invention is a fuel composition
  • a fuel composition comprising a major portion of a hydrocarbon boiling in a gasoline or diesel range and an amount of a modified polyamino alkenyl or alkyl succinimide sufficient to provide dispersancy and/or detergency.
  • the modified polyamino alkenyl or alkyl succinimides of this invention are prepared from a polyamino alkenyl or alkyl succinimide. In turn, these materials are prepared by reacting an alkenyl or alkyl succinic anhydride with a polyamine as shown in reaction (1) below:
  • R is an alkenyl or alkyl group of from 10 to 300 carbon atoms; and R 1 is the remainder of the polyamino moiety.
  • the alkenyl or alkyl group of the succinimide is from 10 to 300 carbon atoms. While the modified succinimides of this invention possess good detergency properties even for alkenyl or alkyl groups of less than 20 carbon atoms, dispersancy is enhanced when the alkenyl or alkyl group is at least 20 carbon atoms. Accordingly, in a preferred embodiment, the alkenyl or alkyl group of the succinimide is at least 20 carbon atoms.
  • succinimide is understood in the art to include many of the amide, imide and amidine species which are also formed by this reaction.
  • the predominant product however is succinimide and this term has been generally accepted as meaning the product of a reaction of an alkenyl substituted succinic acid or anhydride with a polyamine as shown in reaction (1) above.
  • alkenyl or alkyl mono-, bis-succinimides and other higher analogs are included within this term.
  • the preparation of the alkenyl-substituted succinic anhydride by reaction with a polyolefin and maleic anhydride has been described, e.g., U.S. Patents Nos. 3,018,250 and 3,024,195.
  • Such methods include the thermal reaction of the polyolefin with maleic anhydride and the reaction of a halogenated polyolefin, such as a chlorinated polyolefin, with maleic anhydride.
  • Reduction of the alkenyl-substituted succinic anhydride yields the corresponding alkyl derivative.
  • the alkenyl substituted succinic anhydride may be prepared as described in U.S. Patents Nos. 4,388,471 and 4,450,281 which are totally incorporated herein by reference.
  • Polyolefin polymers for reaction with the maleic anhydride are polymers comprising a major amount of C 2 to C 5 mono-olefin, e.g., ethylene, propylene, butylene, isobutylene and pentene.
  • the polymers can be homopolymers such as polyisobutylene as well as copolymers of 2 or more such olefins such as copolymers of: ethylene and propylene, butylene, and isobutylene, etc.
  • copolymers include those in which a minor amount of the copolymer monomers, e.g., 1 to 20 mole percent is a C 4 to C 8 noncon- jugated diolefin, e.g., a copolymer of isobutylene and butadiene or a copolymer of ethylene, propylene and 1,4-hexadiene, etc.
  • a minor amount of the copolymer monomers e.g., 1 to 20 mole percent is a C 4 to C 8 noncon- jugated diolefin, e.g., a copolymer of isobutylene and butadiene or a copolymer of ethylene, propylene and 1,4-hexadiene, etc.
  • the polyolefin polymer usually contains from about 10 to 300 carbon atoms, although preferably 10 to 200 carbon atoms; more preferably 12 to 100 carbon atoms and most preferably 20 to 100 carbon atoms.
  • a particularly preferred class of olefin polymers comprises the polybutenes, which are prepared by polymerization of one or more of 1-butene, 2-butene and isobutene. Especially desirable are polybutenes containing a substantial proportion of units derived from isobutene.
  • the polybutene may contain minor amounts of butadiene which may or may not be incorporated in the polymer. Most often the isobutene units constitute 80%, preferably at least 90%, of the units in the polymer.
  • These polybutenes are readily available commercial materials well known to those skilled in the art. Disclosures thereof will be found, for example, in U.S. Patents Nos. 3,215,707; 3,231,587; 3,515,669; and 3,579,450, as well as U.S. Patent No. 3,912,764. The above are incorporated by reference for their disclosures of suitable polybutenes.
  • alkylating hydrocarbons may likewise be used with maleic anhydride to produce alkenyl succinic anhydride.
  • suitable alkylating hydrocarbons include cyclic, linear, branched and internal or alpha olefins with molecular weights in the range
  • alpha olefins obtained from the thermal cracking of paraffin wax. Generally, these olefins range from 5-20 carbon atoms in length. Another source of alpha olefins is the ethylene growth process which gives even number carbon olefins. Another source of olefins is by the dimerization of alpha olefins over an appropriate catalyst such as the well known Ziegler catalyst. Internal olefins are easily obtained by the isomerization of alpha olefins over a suitable catalyst such as silica.
  • alkenyl or alkyl succinic anhydride are the multiple adducted succinic anhydrides described in U.S. Patent No. 4,234,435 which is incorporated herein in its entirety. These multiple adducted succinic anhydrides are characterized by the presence within their structure of an average of greater than 1 succinic group per each equivalent of alkenyl or alkyl group and preferably an average from greater than 1 to 3.5 succinic groups for each equivalent of alkenyl or alkyl group (substituent group). More preferably, there are an average from at least 1.3 to 3.5 succinic groups for each equivalent of substituent groups and even more preferably from 1.5 to 3.5 succinic groups for each equivalent of substituent group.
  • alkenyl or alkyl group is used herein rather than "substituent group" as used in U.S. Patent No. 4,234,435 but as used herein means the same as “substituent group” and is calculated as described in U.S. Patent No. 4,234,435.
  • the alkenyl or alkyl group has from 10 to about 300 carbon atoms, although preferably from 20 to 100 carbon atoms.
  • Another preferred embodiment for such multiply adducted alkenyl or alkyl succinimides are alkenyl or alkyl groups from 70 to 150 carbon atoms.
  • the polyamine employed to prepare the polyamino alkenyl or alkyl succinimides is preferably polyamine having from 2 to about 12 amine nitrogen atoms and from 2 to about 40 carbon atoms.
  • the polyamine is reacted with an alkenyl or alkyl succinic anhydride to produce the polyamino alkenyl or alkyl succinimide, employed in this invention.
  • the polyamine is so selected so as to provide at least one basic amine per succinimide.
  • a hydroxy hydrocarbyl oxycarbonyl or a hydroxy polyoxyalkylene oxycarbonyl is believed to efficiently proceed through a secondary or primary amine
  • at least one of the basic amine atoms of the polyamino alkenyl or alkyl succinimide must either be a primary amine or a- secondary amine. Accordingly, in those instances in which the succinimide contains only one basic amine, that amine must either be a primary amine or a secondary amine.
  • the polyamine preferably has a carbon-to-nitrogen ratio of from about 1:1 to about 10:1.
  • the polyamine portion of the polyamino alkenyl or alkyl succinimide may be substituted with substituents selected from (A) hydrogen, (B) hydrocarbyl groups of from 1 to about 10 carbon atoms, (C) acyl groups of from 2 to about 10 carbon atoms, and (D) monoketo, monohydroxy, mononitro, monocyano, lower alkyl and lower alkoxy derivatives of (B) and (C).
  • At least one of the substituents on one of the amines of the polyamine is hydrogen, e.g., at least one of the basic nitrogen atoms of the polyamine is a primary or secondary amino nitrogen atom.
  • Hydrocarbyl denotes an organic radical composed of carbon and hydrogen which may be aliphatic, alicyclic, aromatic or combinations thereof, e.g., aralkyl.
  • the hydrocarbyl group will be relatively free of aliphatic unsaturation, i.e., ethylenic and acetylenic, particularly acetylenic unsaturation.
  • the substituted polyamines of the present invention are generally, but not necessarily, N-substituted polyamines.
  • hydrocarbyl groups and substituted hydrocarbyl groups include alkyls such as methyl, ethyl, propyl, butyl, isobutyl, pentyl, hexyl, octyl, etc., alkenyls such as propenyl, isobutenyl, hexenyl, octenyl, etc., hydroxyalkyls, such as 2-hydroxyethyl, 3-hydroxypropyl, hydroxyisopropyl, 4-hydroxybutyl, etc., ketoalkyls, such as 2-ketopropyl, 6-ketooctyl, etc., alkoxy and lower alkenoxy alkyls, such as ethoxyethyl, ethoxypropyl, propoxyethyl, propoxypropyl, 2-(2-ethoxyethoxy)ethyl, 2-(2-(2-ethoxyethoxy)ethoxy ethyl, 3,6,9,12-
  • the acyl groups of the aforementioned (C) substituents are such as propionyl, acetyl, etc.
  • the more preferred substituents are hydrogen, C 1 -C 6 alkyls and C 1 -C 6 hydroxyalkyls.
  • substituted polyamine the substituents are found at any atom capable of receiving them.
  • the substituted atoms e.g., substituted nitrogen atoms, are generally geometrically inequivalent, and consequently the substituted amines finding use in the present invention can be mixtures of mono- and polysubstituted polyamines with substituent groups situated at equivalent and/or inequivalent atoms.
  • the more preferred polyamine finding use within the scope of the present invention is a polyalkylene polyamine, including alkylene diamine, and including substituted polyamines, e.g., alkyl substituted polyalkylene polyamine.
  • the alkylene group contains from 2 to 6 carbon atoms, there being preferably from 2 to 3 carbon atoms between the nitrogen atoms.
  • Such groups are exemplified by ethylene, 1,2-propylene, 2,2-dimethyl-propylene, trimethylene, etc..
  • polyamines examples include ethylene diamine, diethylene triamine, di(tri- methylene)triamine, dipropylene triamine, triethylene tetramine, tripropylene tetramine, tetraethylene pentamine, and pentaethylene hexamine.
  • Such amines encompass isomers such as branched-chain polyamines and the previously mentioned substituted polyamines, including hydrocarbyl-substituted polyamines.
  • polyalkylene polyamines those containing 2-12 amine nitrogen atoms and 2-24 carbon atoms are especially preferred, and the C 2 -C 5 alkylene polyamines are most preferred, in particular, the lower polyalkylene polyamines, e.g., ethylene diamine, dipropylene triamine, etc.
  • the polyamine component also may contain heterocyclic polyamines, heterocyclic substituted amines and substituted heterocyclic compounds, wherein the heterocycle comprises one or more 5-6 membered rings containing oxygen and/or nitrogen.
  • heterocycles may be saturated or unsaturated and substituted with groups selected from the aforementioned (A), (B), (C) and (D).
  • the heterocycles are exemplified by piperazines, such as 2-methylpiperazine, N-(2-hydroxyethyl)piperazine, 1,2-bis-(N-piperazinyl)ethane, and N,N'-bis(N-piperazinyl)piperazine, 2-methylimidazoline, 3-aminopiperidine, 2-aminopyridine, 2-(3-aminoethyl)-3-pyrroline, 3-amino-pyrrolidine, N-(3-aminopropyl)-morpholine, etc.
  • the piperazines are preferred.
  • Typical polyamines that can be used to form the compounds of this invention include the following: ethylene diamine, 1,2-propylene diamine, 1,3-propylene diamine, diethylene triamine, triethylene tetramine, hexamethylene diamine, tetraethylene pentamine, methylamino-propylene diamine, N-(betaaminoethyl)piperazine, N,N'-di(betaaminoethyl)piperazine, N,N'-di(beta-aminoethyl)- imidazolidone-2, N-(beta-cyanoethyl) ethane-1,2-diamine, 1,3,6,9-tetraaminooctadecane, 1,3,6-triamino-9-oxadecane, N-(beta-aminoethyl)diethanolamine, N-methyl-1,2-propanediamine, 2-(2-aminoethy
  • propyleneamines bisaminopropylethylenediamines
  • Propyleneamines are prepared by the reaction of acrylonitrile with an ethyleneamine, for example, an ethyleneamine having the formula H 2 N(CH 2 CH 2 NH) Z H wherein Z is an integer from 1 to 5, followed by hydrogenation of the resultant inter mediate.
  • the product prepared from ethylene diamine an acrylonitrile would be H 2 N(CH 2 ) 3 NH(CH 2 ) 2 NH(CH 2 ) 3 NH 2 .
  • the polyamine used as a reactant in the production of succinimides of the present invention is not a single compound but a mixture in which one or several compounds predominate with the average composition indicated.
  • tetraethylene pentamine prepared by the polymerization of aziridine or the reaction of dichloroethylene and ammonia will have both lower and higher amine members, e.g., triethylene tetramine, substituted piperazines and pentaethylene hexamine, but the composition will be largely tetraethylene pentamine and the empirical formula of the total amine composition will closely approximate that of tetraethylene pentamine.
  • Preparation of the bis- and higher analogs may be accomplished by controlling the molar ratio of the reagents.
  • a product comprising predominantly mono- or bis-succinimide can be prepared by controlling the molar ratios of the polyamine and succinic anhydride.
  • a predominantly mono-succinimide product will be prepared.
  • two moles of an alkenyl or alkyl substituted succinic anhydride are reacted per mole of polyamine, a bis-succinimide is prepared.
  • Higher analogs may likewise be prepared.
  • multiply adducted alkenyl or alkyl succinimide refers to the reaction product of a polyamine with a multiply adducted alkenyl or alkyl succinic anhydride which in turn is an alkenyl or alkyl succinic anhydride characterized by the presence within their structure of an average of greater than 1 succinic group for each equivalent of alkenyl or alkyl group (substituent group).
  • a particularly preferred class of polyamino alkenyl or alkyl succinimides employed in the process of the instant invention may be represented by Formula II:
  • R is alkenyl or alkyl of from 10 to 300 carbon atoms;
  • R 2 is alkylene of 2 to 10 carbon atoms;
  • R 3 is hydrogen, lower alkyl or lower hydroxy alkyl;
  • a is an integer from 0 to 10; and
  • W is -NH 2 or represents a group of Formula III:
  • R is alkenyl or alkyl of from 10 to 300 carbon atoms; with the proviso that when W is the group of Formula III above, then a is not zero and at least one of R 3 is hydrogen.
  • the polyamine employed in preparing the succinimide is often a mixture of different compounds having an average composition indicated as the Formula II. Accordingly, in Formula II each value of R 2 and R 3 may be the same as or different from other R 2 and R 3 .
  • R is alkenyl or alkyl of 10 to 200 carbon atoms and most preferably 20 to 100 carbon atoms.
  • R 2 is alkylene of 2 to 6 carbon atoms and most preferably is either ethylene or propylene.
  • R 3 is hydrogen.
  • a is an integer from 1 to 6.
  • the polyamino alkenyl or alkyl succinimides may be conveniently viewed as being composed of three moieties that is the alkenyl or alkyl moiety R, the succinimide moiety represented by the formula:
  • the preferred alkylene polyamines employed in this reaction are generally represented by the formula:
  • R 2 is an alkylene moiety of 2 to 10 carbon atoms and a is an integer from about 0 to 10.
  • a is an integer from about 0 to 10.
  • the preparation of these alkylene polyamines do not produce a single compound and cyclic heterocycles, such as piperazine, may be included to some extent in the alkylene diamines.
  • the polyamino alkenyl or alkyl succinimides wherein one or more of the nitrogens of the polyamino moiety is substituted with a hydrocarbyl oxycarbonyl, or a hydroxy hydrocarbyl oxycarbonyl wherein said hydrocarbyl contains from 1 to about 20 carbon atoms and said hydroxy hydrocarbyl contains from 2 to about 20 carbon atoms may be prepared by reaction with a cyclic carbonate; by reaction with a linear mono- or poly-carbonate; or by reaction with a suitable chloroformate. Hydroxy poly(oxyalkylene) oxycarbonyl may be formed by reaction with a suitable chloroformate.
  • the products so produced are effective dispersant and detergent additives for lubricating oils and for fuel.
  • Hydrocarbyl as used in describing the hydro- carbyl oxycarbonyl components of this invention, denotes an organic radical composed of carbon and hydrogen which may be aliphatic, aromatic or combinations thereof, e.g., aralkyl.
  • the hydrocarbyl group contains from about 1 to 20 carbon atoms, preferably 2 to 10 carbon atoms and most preferably 2 to 7 carbon atoms.
  • Suitable hydrocarbyls are alkyls such as methyl, ethyl, propyl, butyl, isobutyl, pentyl, hexyl, octyl, etc.; alkenyls such as propenyl, isobutenyl, hexenyl, octenyl, etc.; aralkyl such as benzyl, and the like; aryls such as phenyl, naphthyl, and the like.
  • Hydroxy substituted hydrocarbyl denotes an organic radical composed of carbon and hydrogen containing 1 to 6 hydroxy groups, preferably 1 to 3, more preferably 1 to 2 hydroxy groups and most preferably 1 hydroxy group. It is also possible that some keto and aldehyde groups may be present in these hydroxy substituted hydrocarbyls. In the preferred embodiment the hydroxy hydrocarbyl does not contain ketone or aldehyde groups.
  • the hydroxy substituted hydrocarbyl group contains from 2 to 20 carbon atoms, preferably 2 to 10 carbon atoms and most preferably 2 to 7 carbon atoms.
  • Suitable hydroxy hydrocarbyls are hydroxy alkyls such as 2-hydroxyethyl, 3-hydroxypropyl, hydroxyisopropyl, 4-hydroxybutyl, 6-hydroxyhexyl, 2,3-dihydroxypropyl and the like. Some hydroxy alkyls may also be termed "hydroxyalkylene" such as 3-hydroxypropylene (HOCH 2 CH 2 CH 2 -) and are included within the term hydroxy alkyls defined above.
  • Other suitable hydroxyhydrocarbyls are hydroxy aralkyls such as 3-hydroxy-2-phenylpropyl
  • Hydroxy poly (oxyalkylene) as used in describing the hydroxy poly (oxyalkylene) oxycarbonyl components of this invention, denotes a polymer containing from 2 to 30 C 2 -C 5 oxyalkylene units and may be represented by the formula:
  • alkylene is a C 2 -C 5 alkyklene group and s is an integer from 2 to 30.
  • the polyamino alkenyl or alkyl succinimide wherein one or more of the nitrogens of the succinimide is substituted with a hydroxy hydrocarbyl oxycarbonyl may be prepared by reaction of a polyamino alkenyl or alkyl succinimide with a cyclic carbonate. This reaction is conducted at a temperature sufficient to cause reaction of the cyclic carbonate with the polyamino alkenyl or alkyl succinimide. In particular, reaction temperatures of from about 0°C to about 250°C are preferred with temperatures of from about 100°C to 200°C being more preferred and temperatures of from 150° to 180°C are most preferred.
  • the reaction may be conducted neat - that is, both the alkenyl or alkyl succinimide and the cyclic carbonate are combined in the proper ratio, either alone or in the presence of a catalyst, such as an acidic, basic or Lewis acid catalyst, and then stirred at the reaction temperature.
  • a catalyst such as an acidic, basic or Lewis acid catalyst
  • suitable catalysts include, for instance, phosphoric acid, boron trifluoride, alkyl or aryl sulfonic acid, alkali or alkaline carbonate.
  • the reaction may be conducted in a diluent.
  • the reactants may be combined in a solvent such as toluene, xylene, oil or the like, and then stirred at the reaction temperature. After reaction completion, volatile components may be stripped off.
  • a diluent it is preferably inert to the reactants and products formed and is generally used in an amount sufficient to insure efficient stirring.
  • Water which can be present in the polyamino alkenyl or alkyl succinimide, may be removed from the reaction system either before or during the course of the reaction via azeotroping or distillation. After reaction completion, the system can be stripped at elevated temperatures (100°C to 250°C) and reduced pressures to remove any volatile components which may be present in the product.
  • Another embodiment of the above process is a continuous system in which the alkenyl or alkyl succinic anhydride and polyamine are added at the front end of the system while the cyclic carbonate is added further downstream in the system.
  • the cyclic carbonate may be added at any time after mixing of the alkenyl or alkyl succinic anhydride with the polyamine has occurred.
  • the organic carbonate is added within two hours after mixing of the alkenyl or alkyl succinic anhydride with the polyamine, preferably after the major portion of the amine has reacted with the anhydride.
  • the reaction temperature may be adjusted to maximize reaction efficiency. Accordingly, the temperature employed in the reaction of the alkyl or alkenyl succinic anhydride with a polyamine may be the same as or different from that which is maintained for the reaction of this resulting product with the cyclic carbonate. In such a continuous system, the reaction temperature is generally between 0-250°C; preferably between 125-200°C; and most preferably between 150-180°C.
  • another aspect of the instant invention is a continuous process which comprises (a) contacting at a temperature sufficient to cause reaction an alkenyl or alkyl succinic anhydride with a polyamine; and (b) then contacting at a temperature sufficient to cause reaction the product of (a) above with a cyclic carbonate.
  • Mole ratios of the cyclic carbonate to the basic amine nitrogen of the polyamino alkenyl or alkyl succinimide employed in the process of this invention are generally in the range of from about 0.2:1 to about 10:1; although preferably from about 0.5:1 to about 5:1; more preferably from about 1:1 to 3:1 another preferred embodiment is 2:1.
  • the reaction is generally complete from with 0.5 to 10 hours.
  • Preferred cyclic carbonates include:
  • R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are independently selected from hydrogen or lower alkyl of 1 to 2 carbon atoms; R 10 is either hydrogen or hydroxy; and n is an integer from 0 to 1.
  • Preferred cyclic carbonates for use in this invention are those of formula 1 above.
  • Preferred R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are either hydrogen or methyl. Most preferably R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are hydrogen when n is one. R 8 is most preferably hydrogen or methyl while R 4 , R 5 , and R 9 are hydrogen when n is zero.
  • suitable cyclic carbonates for use in this invention 1,3-dioxolan-2- one(ethylene carbonate); 4-methyl-1,3-dioxolan-2-one(propylene carbonate); 4-hydroxymethyl-1,3-dioxolan-2-one;
  • 1,3-dioxolan-2-one 1,3-dioxolan-2-one; 4,5-diethyl-1,3-dioxolan-2-one; 4,4- diethyl-1,3-dioxolan-2-one; 1,3-dioxan-2-one; 4,4- dimethyl-1,3-dioxan-2-one; 5,5-dimethyl-1,3-dioxan-2-one;
  • Suitable cyclic carbonates may be prepared from sacchrides such as sorbitol, glucose, fructose, galactose and the like and from visconal diols prepared from C 1 -C 30 olefins by methods known in the art.
  • cyclic carbonates are commercially available such as 1,3-dioxolan-2-one or 4-methyl1,3-dioxolan-2-one.
  • Cyclic carbonates may be readily prepared by known reactions. For example, reaction of phosgene with a suitable alpha alkane diol or an alkan-1,3-diol yields a carbonate for use within the scope of this invention as for instance in U.S. 4,115,206 which is incorporated herein by reference.
  • the cyclic carbonates useful for this invention may be prepared by transesterif ication of a suitable alpha alkane diol or an alkan-1,3-diol with, e.g., diethyl carbonate under transesterification conditions. See, for instance, U.S. Patent Nos. 4,384,115 and 4,423,205 which are incorporated herein by reference for their teaching of the preparation of cyclic carbonates.
  • alpha alkane diol means an alkane group having two hydroxyl substituents wherein the hydroxyl substituents are on adjacent carbons to each other.
  • alpha alkane diols include 1,2-propanediol, 2,3-butanediol and the like.
  • alkan-1,3-diol means an alkane group having two hydroxyl substituents wherein the hydroxyl substituents are beta substituted. That is, there is a methylene or a substituted methylene moiety between the hydroxyl substituted carbons.
  • alkan-1,3-diols examples include propan-1,3-diol, pentan-2,4-diol and the like.
  • hydroxy hydrocarbyl oxycarbonyl refers to the group hydroxy hydrocarbyl-OC-; the term “hydrocarbyloxy carbonyl” refers to the group
  • the term "molar charge of cyclic carbonate (or chloroformate or linear carbonate) to the basic nitrogen of a polyamino alkenyl or alkylsuccinimide” means that the molar charge of cyclic carbonate (or chloroformate or linear carbonate) employed in the reaction is based upon the theoretical number of basic nitrogens contained in the succinimide.
  • TETA triethylene tetraamine
  • a molar charge of 1 would require that a mole of cyclic carbonate (or chloroformate or linear carbonate) be added for each basic nitrogen or in this case 3 moles of cyclic carbonate for each mole of monosuccinimide prepared from TETA.
  • the alpha alkane diols used to prepare the 1,3- dioxolan-2-ones employed in this invention, are either commercially available or may be prepared from the corresponding olefin by methods known in the art.
  • the olefin may first react with a peracid, such as peroxyacetic acid or hydrogen peroxide to form the corresponding epoxide which is readily hydrolyzed under acid or base catalysis to the alpha alkane diol.
  • the olefin is first halogenated to a dihalo derivative and subsequently hydrolyzed to an alpha alkane diol by reaction first with sodium acetate and then with sodium hydroxide.
  • the olefins so employed are known in the art.
  • the alkan-1,3-diols, used to prepare the 1,3-dioxan-2-ones employed in this invention are either commercially available or may be prepared by standard techniques, e.g., derivatizing malonic acid.
  • 4-Hydroxymethyl 1,3-dioxolan-2-one derivatives and 5-hydroxy-1,3-dioxan-2-one derivatives may be prepared by employing glycerol or substituted glycerol in the process of U.S. Patent 4,115,206.
  • the mixture so prepared may be separated, if desired, by conventional techniques. Preferably the mixture is used as is.
  • 5,5-Dihydroxymethyl-1,3-dioxan-2-one may be prepared by reacting an equivalent of pentaerythritol with an equivalent of either phosgene or diethylcarbonate (or the like) under transesterif ication conditions.
  • 5-hydroxymethyl-5-methyl-1,3-dioxan-2-one may be prepared by reacting an equivalent of trimethylolethane with an equivalent of either phosgene or diethylcarbonate (or the like) under transesterification conditions.
  • Spiro[1,3-oxa-2-cyclohexanone-5,5'-1',3'-oxa-2'-cyclohexanone] may be prepared by reacting an equivalent of pentaerythritol with two equivalents of either phosgene or diethylcarbonate (or the like) under transesterification conditions.
  • Cyclic carbonates of Formula I are used to illustrate the reaction of a cyclic carbonate with a polyamino alkenyl or alkyl succinimide. It is to be understood that the other cyclic carbonates employed in this invention react similarly. Cyclic carbonates may react with the primary and secondary amines of a polyamino alkenyl or alkyl succinimide to form two types of compounds. In the first instance, strong bases, including unhindered amines such as primary amines and some secondary amines, react with an equivalent of cyclic carbonate to produce a carbamic ester as shown in reaction (2) below:
  • R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and n are as defined above and R 11 is the remainder of a polyamino alkenyl or alkyl succinimide.
  • the amine nitrogen has been rendered nonbasic by formation of the carbamate, V.
  • hindered bases such as hindered secondary amines, may react with an equivalent of the same cyclic carbonate to form a hydroxyalkyleneamine linkage with the concomitant elimination of CO 2 as shown below in reaction (3): ( 3 )
  • R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 1 1 and n are as defined above and R 12 is an alkyl or alkylene linking group which hinders the amine.
  • R 12 is an alkyl or alkylene linking group which hinders the amine.
  • the hydroxyalkyleneamine products of reaction (3) retain their basicity.
  • R 4 , R 5 , R 6 and R 7 are as defined above. (See for instance U.S. Patents Nos. 3,367,943 and 3,377,111).
  • reaction (2) a determination of whether the carbonate addition follows reaction (2) or reaction (3) could be made by monitoring the AV (alkalinity value or alkalinity number - refers to the amount of base as milligrams of KOH in 1 gram of a sample) of the product. Accordingly, if the reaction proceeded entirely via reaction (2) above, a reaction product prepared by reacting an equivalent of carbonate for each basic nitrogen should yield an AV of zero. That is to say that all the basic amines in the polyamine moiety have been converted to nonbasic carbamates.
  • AV alkalinity value or alkalinity number - refers to the amount of base as milligrams of KOH in 1 gram of a sample
  • alkylene polyamines such as triethylene tetraamine and tetraethylene pentamine (e.g., tetraethyleneperitaamine-TEPA and tri- ethylenetetramine-TETA), contain tertiary amines (piperazines, etc.) which may account for as much as 30% of the basic nitrogen content.
  • tertiary amines piperazines, etc.
  • TETA triethylenetetramine
  • reaction 4a allows for additional carbonate to add to the hydroxyl group of product IX to form a hydroxy tri (oxyalkylene) carbamate as shown in reaction 4(b) below: IX + I ⁇
  • poly (oxyalkylene) polymers of the carbamic esters and the hydroxyhydrocarbylamine derivatives are expected. It is expected that use of the spiro[1,3-oxa-2- cyclohexanone-5,5'-1',3'-oxa-2'-cyclohexanone] may yield internally cyclized products and also bring about cross- linking between two succ in imides .
  • Linear Mono- or Polycarbonates Linear carbonates react with a basic nitrogen of a polyamino alkenyl or alkyl succinimide to form car- bamates.
  • Suitable linear carbonates include both monocarbonates of formula XIII and polycarbonates of formula XIV:
  • R 14 is hydrocarbyl of from 1 to 10 carbon atoms
  • R 1 5 is hydroxy hydrocarbyl of from 2 to 10 carbon atoms
  • R 16 is a divalent hydrocarbyl of from 2 to
  • n is preferably an integer from 1 to
  • Monocarbonates, XIII are believed to react with primary or secondary amines of a polyamino alkenyl or alkyl succinimide, with the concommittant elimination of the alcohol, R 14 OH, as shown in reaction (6) below:
  • R 1 1 and R 14 are as defined above.
  • Reaction (6) is conducted by contacting the monocarbonate with a polyamino alkenyl or alkyl succinimide.
  • the reaction is conducted at a temperature sufficient to cause reaction of the monocarbonate with the polyamino alkenyl or alkyl succinimide.
  • reaction temperatures of from about 100°C to about 250°C are preferred with temperatures of from about 150°C to 250°C being most preferred.
  • the reaction may be conducted neat - that is, both the polyamino alkenyl or alkyl succinimide and the carbonate are combined in the proper ratio, either alone or in the presence of a catalyst, such as an acidic, basic or Lewis acid catalyst, and then stirred at the reaction temperature.
  • a catalyst such as an acidic, basic or Lewis acid catalyst
  • suitable catalysts include, for instance, phosphoric acid, boron trifluoride, alkyl or aryl sulfonic acid, alkali or alkaline carbonate.
  • the reaction may be conducted in a diluent.
  • the reactants may be combined in a solvent such as toluene, xylene, oil or the like, and then stirred at the reaction temperature. After reaction completion, volatile components may be stripped off.
  • a diluent it is preferably inert to the reactants and products formed and is generally used in an amount sufficient to insure efficient stirring.
  • Water which can be present in the polyamino alkenyl or alkyl succinimide, may be removed from the reaction system either before or during the course of the reaction via azeotroping or distillation. After reaction completion, the system can be stripped at elevated temperatures (100°C to 250°C) and reduced pressures to remove any volatile components which may be present in the product.
  • Another embodiment of the above process is acontinuous flow system in which the alkenyl or alkyl succinic anhydride and polyamine are added at the front end of the flow while the hydrocarbyl carbonate is added further downstream in the system.
  • Mole ratios of the hydrocarbyl carbonate to the basic amine nitrogen of the polyamino alkenyl or alkyl succinimide employed in the process of this invention are generally in the range of from about 0.2:1 to about 1:1; preferably 0.5:1 to about 1:1 and most preferably 0.7:1 to about 1:1.
  • the reaction is generally complete from within
  • Suitable monocarbonates, XIII may be prepared by transesterifying diethyl carbonate or a similar material using conditions well known in the art. Suitable monocarbonates include dimethyl carbonate, diethyl carbonate, di-n-propyl carbonate, diisopropylcarbonate, diphenyl carbonate, di-n-butyl carbonate, dibenzyl carbonate, and the like.
  • Linear polycarbonates are of the general formula:
  • the carbamates of formula XVIII may be post-treated with a cyclic carbonate such as ethylene carbonate to form a hydroxy polyoxyalkylene derivative similar to that of formula X above.
  • Reaction (7) is conducted at a temperature sufficient to cause reaction of the polycarbonate, XIV, wi th the polyami no alkenyl or alkyl succ inimide , IV.
  • reaction temperatures of from about 0°C to about 250°C are preferred with temperatures of from about 100°C to 200°C being most preferred.
  • the reaction may be conducted neat - that is, both the polyamino alkenyl or alkyl succinimide and the polycarbonate are combined in the proper ratio, either alone or in the presence of a catalyst, such as an acidic, basic or Lewis acid catalyst, and then stirred at the reaction temperature.
  • a catalyst such as an acidic, basic or Lewis acid catalyst
  • suitable catalysts include, for instance, phosphoric acid, boron trifluoride, alkyl or aryl sulfonic acid, alkali or alkaline carbonate.
  • the reaction may be conducted in a diluent.
  • the reactants may be combined in a solvent such as toluene, xylene, oil or the like, and then stirred at the reaction temperature. After reaction completion, volatile components may be stripped off.
  • a diluent it is preferably inert to the reactants and products formed and is generally used in an amount sufficient to insure efficient stirring.
  • Water which can be present in the polyamino alkenyl or alkyl succinimide, may be removed from the reaction system either before or during the course of the reaction via azeotroping or distillation. After reaction completion, the system can be stripped at elevated temperatures (100°C to 250°C) and reduced pressures to remove any volatile components which may be present in the product.
  • Another embodiment of the above process is a continuous flow system in which the alkenyl or alkyl succinic anhydride and polyamine are added at the front end of the flow while the polycarbonate is added further down-stream in the system.
  • Mole ratios of the individual carbonate units of polycarbonate to the basic amine nitrogen of the polyamino alkenyl or alkyl succinimide employed in the process of this invention are generally in the range of from about 0.1:1 to about 5:1 although preferably from about 0.5:1 to about 1:1.
  • the reaction is generally complete from within 0.5 to 10 hours.
  • Suitable polycarbonates may be prepared as described in U.S. Patent No. 4,423,205. This patent is incorporated herein by reference for its teaching of the preparation of polycarbonates.
  • Preferred polycarbonates for use in this invention are those wherein R 15 is hydroxyalkylene and R 16 is alkylene wherein alkylene is from 2 to 10 carbon atoms; preferably 2 to 5 carbon atoms.
  • Other preferred polycarbonates are those wherein R 15 is HO-Aryl-R 17 -Aryl- and R 16 is -Aryl-R 17 -Aryl- wherein R 17 is alkylene of from 2 to 5 carbon atoms and aryl is a C 6 to C 10 aryl.
  • Suitable aryls include benzyl and naphthyl.
  • Chloroformates and other haloformates react with a primary or secondary amine nitrogen of a polyamino alkenyl or alkyl succinimide to form carbamates.
  • Suitable chloroformates include hydrocarbyl chloroformates of formula XIX below; hydroxy protected hydrocarbyl chloroformates of formula XX below and hydroxy protected poly (oxyalkylene) chloroformates of formula XXI:
  • w is an integer from 1 to 6;
  • R 1 8 is hydrocarbyl of from 1 to 20 carbon atoms,
  • R 19 is hydrocarbyl of 2 to 20 carbon atoms,
  • R 20 is a hydroxy protecting group, alkylene is a C 2 -C 5 alkylene group and s is an integer from 2 to
  • R 1 1 and R 18 are as defined above.
  • Reaction (9) is conducted by contacting the chloroformate, XIX (or XX or XXI), with the polyamino alkenyl or alkyl succinimide, IV.
  • the reaction may be conducted neat or in a suitable inert diluent. Suitable diluents include ethyl acetate, toluene, xylene, oil and the like.
  • An organic base such as pyridine, triethylamine and the like may be added to the reaction to scavenge the acid generated. However, the generated acid is preferably removed by an alkaline water wash (pH of from 8-9) or an alkaline brine wash (pH 8-9) of the reaction solution after reaction completion without the need of added base.
  • the reaction is generally conducted at from -78°C to 50°C with 0°-30°C being preferred.
  • chloroformate XX or XXI is employed, and the protecting R 20 group is trichloroacetate, use of lower temperatures, i.e., -78°C to 0°C help prevent possible side products from forming and may be preferred for this purpose.
  • the reaction is generally complete from within 0.5 to 24 hours.
  • the polyamino moiety of the alkenyl or alkyl succinimide contains hydroxyalkyl substitution, it is preferable to conduct reaction (9) at a sufficiently low temperature to prevent reaction of the chloroformate with the hydroxy group resulting in carbonate formation.
  • any carbonate so formed from the hydroxyalkyl group during the chloroformate reaction may itself react with a primary or secondary amino nitrogen of the succinimide or may be readily removed by posttreating the product with an alkanol (e.g., ethanol) under transesterif ication conditions.
  • an alkanol e.g., ethanol
  • the hydroxy protecting group, R 20 used in chloroformate, XX and XXI, is any acceptable hydroxy protecting groups which do not contain a functionality which is reactive with a chloroformate or an amine of the succinimide under the reaction conditions. Suitable protecting groups include benzyl, carbobenzoxy (C 6 H 5 CH 2 OC-),
  • trichloroacetyl (CCl 3 C-) and the like.
  • the identity of the particular protecting group is not critical provided it can be readily removed from the hydroxy group after reaction (9) is completed.
  • trichloroacetyl may be removed by an alkaline brine wash (pH of from 8-9); by addition of a dialkylamine (e.g., dimethylamine into the reaction medium; or di-n-butylamine) or by an aqueous solution of tetrahydrofuran containing approximately 30% water at a pH 9-10, conducted at the completion of reaction (9) as shown in reaction (10) below:
  • R 20 protecting group XXIII XXIV More extreme reaction conditions (i.e. higher temperature or pH >9-10) may result in product decomposition. Removal of other R 20 protecting groups is well known in the art. For example, benzyl and carbobenzoxy protecting groups may be readily removed by hydrogenation using a suitable catalyst such as palladium on carbon. Similarly, carbobenzoxyprotecting groups may also be removed by trifluoroacetic acid.
  • XIX, XX, or XXI is added to the reaction it will react with any available primary or secondary amine of the polyamine alkenyl or alkyl succinimide and convert these to carbamates.
  • maximum carbamate formation in the polyamino alkenyl or alkyl succinimide can be obtained by employing a molar charge of chloroformate to the theoretical bas ic nitrogen of the alkenyl or alkyl succinimide of from 0.7:1 to about 1:1. In some cases, a slight excess of chloroformate may be employed to enhance reaction rate.
  • Suitable chloroformates of formula XIX include C 1 to C 20 alkyl chloroformates prepared from the corresponding alcohol by reaction with phosgene. The alcohols are either commercially available or may be readily prepared by reduction of the corresponding carboxylic acid by art recognized techniques.
  • the protecting group R 20 is trichloroacetyl although it is understood that other suitable protecting groups may be similarly employed.
  • Reaction (11) is a conventional esterification reaction and is conducted by combining the diol, XXV, with the acid XXVI, to yield the monester, XXVII.
  • an excess of diol, XXV is employed.
  • from 1.1 to 4 equivalents of diol, XXV, and preferably 2 equivalents per equivalent of acid XXVI are employed in reaction (11) although larger excesses may be employed.
  • the reaction may be conducted neat or in a suitable diluent such as toluene, benzene and the like. The water generated during the reaction may be readily removed via a Dean-Stark trap.
  • the product ester, XXVII may be isolated by conventional techniques such as chromatography, filtration and the like.
  • the monoester, XXVII may be prepared by forming the diester of glycol XXV and then hydrolyzing one of the esters to the alcohol to form monoester XXVII.
  • Reaction (12) is conducted by adding the ester, XXVII, to a suitable inert diluent such as toluene, benzene and the like. Phosgene, XXVIII, is then added to the system over a period of time. Generally, an excess of phosgene is employed. In particular, from approximately 1.1-2.5 equivalents of phosgene is added per equivalent of ester, XXVII. The reaction is conducted at from -10° to 10°C and is generally complete from within 1/2 to 12 hours. If it is necessary to prevent formation of side products, the ester, XVII, may be slowly added to an excess of phosgene XXVIII.
  • a suitable inert diluent such as toluene, benzene and the like.
  • Phosgene, XXVIII is then added to the system over a period of time. Generally, an excess of phosgene is employed. In particular, from approximately 1.1-
  • the chloroformate, XXIX may be isolated by conventional techniques such as distillation but preferably the system is stripped of a portion of the inert diluent which also removes the hydrochloride gas generated. The product XXIX, and the remaining diluent are then used as is in reaction (9) above.
  • the glycol, XXV is either commercially available or may be readily prepared from art recognized techniques.
  • the chloroformate, XX is prepared similarly as to reactions (11) and (12) above. However, it is noted that excess polyol in these reactions is not necessary since all but one of the hydroxy groups of the polyol should be protected. Accordingly, if the polyol contains 4 hydroxy groups, three of these should be protected. This can be accomplished by using 3 equivalents of the protecting agent such as trichloroacetic acid.
  • the triester may be prepared by first forming the tetraester and then hydrolyzing one of these esters to a hydroxy group to form the triester. In any case, a mixture is obtained from both procedures and the desired product being isolated by conventional techniques (i.e., chromatography). Polyols are either commercially available (i.e. glycerol, pentaerythritol, etc.) or may be readily prepared by art recognized techniques.
  • Chloroformates of formula XXI are prepared similarly as those of formula XX by substituting a poly(oxyalkylene) glycol, XXX, in reactions (11) and (12) above.
  • alkylene and s are as defined above.
  • the poly(oxyalkylene) glycol materials, XXX are the addition polymers of lower aliphatic oxides such as ethylene oxide, propylene oxide, the butylene oxides and the pentylene oxides and are prepared by employing a glycol such as ethylene glycol, propylene glycol and the like under polymerization conditions. These materials are commercially available or may be readily prepared.
  • a s ingle type of alkylene oxide may be employed, e.g., propylene oxide, in which case the product is a homopolymer, e.g., a poly(oxypropylene) propanol.
  • copolymers are equally satisfactory and random copolymers are readily prepared by contacting the hydroxyl-containing compound with a mixture of alkylene oxides, such as a mixture of propylene and butylene oxides.
  • Block copolymers of oxyalkylene units also provide satisfactory poly(oxyalkylene) polymers for the practice of the present invention.
  • poly (oxyalkylene) polymers are mixtures of compounds that differ in polymer chain length. However, their properties closely approximate those of the polymer represented by the average composition and molecular weight.
  • hydroxy alkyl groups may be introduced into the modified succinimides of this invention by addition of a chloroalkanol (e.g., chloroethanol) provided the succinimide retains some basic nitrogen.
  • a chloroalkanol e.g., chloroethanol
  • the chloroalkanol will react with basic nitrogen to yield the hydroxy alkyl group. This reaction may also produce some quaterinized nitrogen products but this may be minimized by controlling the reaction conditions such as by limiting the amount of chloroalkanol added.
  • the hydroxy hydrocarbyl carbamates may be prepared by reacting the succinimide with an epoxide or hydrocarbyl hydroxy chloride in the presence of CO 2 . Accordingly, by employing chloroformate, XIX, XX, or XXI, and a polyamino alkenyl or alkyl succinimide of formula II above in the above reactions, compounds of the following formula are produced.
  • R is alkenyl or alkyl of from 10 to 300 carbon atoms
  • R 2 is alkylene of from 2 to 10 carbon atoms
  • R 21 is hydrogen; lower alkyl of from 1 to 6 carbon atoms, lower hydroxy alkyl of from 1 to 6 carbon atoms,
  • hydrocarbyl is a hydrocarbyl group of from 2 to 20 carbon atoms
  • alkylene-O is a C 2 -C 5 oxyalkylene and s is an integer from 2 to 30; a is an integer of from 0 to 10; and T is -NH 2 ,
  • R is alkenyl or alkyl of from about 12 to 100 carbon atoms
  • R 2 is alkylene of from 2 to 6 carbon atoms
  • a is an integer of from 1 to 6
  • R 21 is
  • t is an integer of from 1 to 6, more preferably 1 to 3, most preferably 1.
  • Carbon atoms having 2 hydroxy groups are hemiketals which readily lose water to form ketones (or aldehydes).
  • t is 2 or more then the hydroxy groups are not on the same carbon atom.
  • the carbon atom attached to the carbamate cannot be substituted with hydroxy since such hydroxy substitution would require that the starting alcohol XXV (or its equivalent if t is greater than 1) be a hemiketal which is not within the scope of this invention. Accordingly, when more than one hydroxy group is contained in the hydroxyhydrocarbyl group, no more than one hydroxy group is attached to the same carbon atom and the number of carbon atoms is minimally one geater than the number of hydroxy groups.
  • the hydroxy hydrocarbyl carbamates of formula V, XVIII, XXIII and the like may be post-treated with an alkenyl or alkyl succinic anhydride of the formula:
  • R is alkenyl or alkyl of from about 10 to 300 carbon atoms.
  • the reaction is generally conducted by combining the hydroxy hydrocarbyl carbamate and the alkenyl or alkyl succinic anhydride.
  • the reaction may be conducted neat but preferably on an inert diluent such as toluene, xylene, oil or the like is employed.
  • the reaction is generally conducted at from 50° to 250°C , preferably 100-200°C and most preferably 150-180°C and is generally complete from within 1 to 24 hours.
  • the system can be stripped at elevated temperatures and reduced pressures to remove any volatile components which may be present in the product.
  • modified succinimides of this invention can also be reacted at a temperature sufficient to cause reaction with boric acid or a similar boron compound to form borated dispersants having utility within the scope of this invention.
  • boric acid boron acid
  • suitable boron compounds include boron oxides, boron halides and esters of boric acid.
  • from about 0.1 equivalents to 10 equivalents of boron compound to the modified succinimide may be employed.
  • the modified polyamino alkenyl or alkyl succinimides of this invention are useful as detergent and dispersant additives when employed in lubricating oils.
  • the modified polyamino alkenyl or alkyl succinimide additive is usually present in from 0.2 to 10 percent by weight to the total composition and preferably at about 0.5 to 5 percent by weight.
  • the lubrieating oil used with the additive compositions of this invention may be mineral oil or synthetic oils of lubricating viscosity and preferably suitable for use in the crankcase of an internal combustion engine.
  • Crankcase lubricating oils ordinarily have a viscosity of about 1300 CSt 0°F (-17.8°C) to 22.7 CSt at 210°F (99°C).
  • the lubricating oils may be derived from synthetic or natural sources.
  • Mineral oil for use as the base oil in this invention includes paraffinic, naphthenic and other oils that are ordinarily used in lubricating oil compositions.
  • synthetic oils include both hydrocarbon synthetic oils and synthetic esters.
  • Useful synthetic hydrocarbon oils include liquid polymers of alpha olefins having the proper viscosity. Especially useful are the hydrogenated liquid oligomers of C 6 to C 12 alpha olefins such as 1-decene trimer.
  • alkyl benzenes of proper viscosity such as didodecyl benzene
  • useful synthetic esters include the esters of both monocarboxylic acid and polycarboxylic acids as well as monohydroxy alkanols and polyols. Typical examples are didodecyl adipate, pentaerythritol tetracaproate, di-2-ethylhexyl adipate, dilaurylsebacate and the like.
  • Complex esters prepared from mixtures of mono and dicarboxylic acid and mono and dihydroxy alkanols can also be used.
  • Blends of hydrocarbon oils with synthetic oils are also useful. For example, blends of 10 to 25 weight percent hydrogenated 1-decene trimer with 75 to 90 weight percent 150 SUS (100°F) 32 CSt (38°C) mineral oil gives an excellent lubricating oil base.
  • Additive concentrates are also included within the scope of this invention.
  • the concentrates of this invention usually include from about 90 to 10 weight percent of an oil of lubricating viscosity and from about 10 to 90 weight percent of the complex additive of this invention.
  • the concentrates typically contain sufficient diluent to make them easy to handle during shipping and storage.
  • Suitable diluents for the concentrates include any inert diluent, preferably an oil of lubricating viscosity, so that the concentrate may be readily mixed with lubricating oils to prepare lubricating oil compositions.
  • Suitable lubricating oils which can be used as diluents typically have viscosities in the range from about 35 to about 500
  • additives which may be present in the formulation include rust inhibitors, foam inhibitors, corrosion inhibitors, metal deactivators, pour point depressants, antioxidants, and a variety of other well-known additives.
  • modified succinimides of this invention may be employed as dispersants and detergents in hydraulic fluids, marine crankcase lubricants, two cycle engine lubricants and the like.
  • the modified succinimide is added at from about 0.1 to 10 percent by weight to the oil. Preferably, at from 0.5 to 5 weight percent.
  • the proper concentration of the additive necessary in order to achieve the desired detergency is dependent upon a variety of factors including the type of fuel used, the presence of other detergents or dispersants or other additives, etc.
  • the range of concentration of the additive in the base fuel is 10 to 10,000 weight parts per million, preferably from 30 to 2,000 weight parts per million, and most preferably from 30 to 700 parts per million of the modified succinimide per part of base fuel. If other detergents are present, a lesser amount of the modified succinimide may be used.
  • the modified succinimide additives of this invention may be formulated as a fuel concentrate, using an inert stable oleophilic organic solvent boiling in the range of about 150° (65.6°C) to 400°F (204.4°C).
  • an aliphatic or an aromatic hydrocarbon solvent is used, such as benzene, toluene, xylene or higher-boiling aromatics or aromatic thinners.
  • Aliphatic alcohols of about 3 to 8 carbon atoms, such as isopropanol, isobutylcarbinol, n-butanol and the like, in combination with hydrocarbon solvents are also suitable for use with the fuel additive.
  • the amount of the additive will be ordinarily at least 10 percent by weight and generally not exceed 70 percent by weight and preferably from 10 to 25 weight percent.
  • Example 2 To a 5-liter reaction flask fitted with a stirrer, Dean-Stark trap, condensor and nitrogen inlet, was charged 2000 g of a succ
  • the succinimide was warmed to 150°C, 29.9 g ethylene carbonate was added, and the mixture stirred and heated at 150°C under N 2 for 4 hours.
  • the succinimide was warmed to 170°C and 171 g ethylene carbonate added over a period of about 5 minutes.
  • Example 10 To a 1-liter reaction flask was charged 500 g succinimide dispersant composition of Example 4. This material was then stripped to 170°C and 5 mm Hg to remove 1.5 g entrained water. 56.8 g Ethylene carbonate was then added over a 2-minute period and the reaction mixture stirred and heated at 170°C under N 2 for 4 hours.
  • Example 13 To a 500-ml reaction vessel was charged 264 g of an approximately 50% solution of polyisobutenyl succinic anhydride in diluent oil (where the polyisobutenyl group has a number average molecular weight of about 950) and 11.8 g tetraethylenepentamine (a commercial product containing a mixture of poly
  • 9.5 g of tetraethylene pentaamine tetraethylene pentaamine
  • succinimides include the reaction product of either polyisopropenyl succinic anhydride or polyisobutenyl succinic anhydride with bisaminopropylethylene diamine and the reaction product of a hydrogenated polyisobutenyl succinic anhydride with tetraethylene pentamine.
  • pentaerythritol carbonate spiro[1,3-oxa-2-cyclohexanone-5,5'-1',3'-oxa-2'-cyclohexanone]
  • Example 21 A linear polyethylene carbonate was prepared according to U.S. Patent 3,248,414.
  • a stirred steel autoclave was charged with 12.4 g ethylene glycol, 274 g ethylene carbonate, and 0.4 g potassiium carbonate.
  • the temperature was raised to 200°C and held there for 24 hours.
  • the pressure in the vessel rose from 155 psi to 1300 psi and was constant at 1300 psi for at least the last 5 hours of the reaction.
  • the reactor temperature was lowered to 115-120°C and the reaction gases were vented.
  • the product was then stripped under vacuum to 165-170°C to remove excess ethylene carbonate. Recovered 158.9 g product haivng an hydroxyl number of 157 and containing 14.9 weight percent CO 2 .
  • Example 22 A stirred steel autoclave was charged with 12.4 g ethylene glycol, 274 g ethylene carbonate, and 0.4 g potassiium carbonate. The temperature was raised to 200°C and
  • Example 26 To a 250 ml, 3-necked
  • Example 27 To a 500 ml, 3-necked flask was added 5.1 g of the polycarbonate resin described in Example 24 and 100 g p-dioxane. The solvent was refluxed until all the resin had dissolved. 46.4 g of the bissuccinimide dispersant composition of Example 4 was then added and refluxing continued for another 21 hours. The reaction mixtures was then stripped to remove dioxane and heated to 180
  • This succinimide was warmed to 170°
  • Example 41 To a 3-liter, 3-necked flask is charged 1,250 g of the monosuccinimide dispersant composition of Example 36. Afterwards, 276 g of tetradecyl chloroformate (prepared by reacting 1-tetradecanol with phosgene) is slowly added to the reaction system at a temperature from 20°-25°C. The reaction system is stirred at this temperature for 2 hours at which time the reaction solution is added to 250 hydrocarbon thinner which is a mixture of aromatics, paraffins, and naphthenes. The organic solution is washed with brine and then stripped to remove volatiles to yield a dispersant product containing tetradecyl carbamate functionalities.
  • tetradecyl chloroformate prepared by reacting 1-tetradecanol with phosgene
  • Example 42 To a 5-liter, 3-necked flask is charged 1,250 g of the monosuccinimide dispersant composition of Example 36. Afterwards, 1,440 g of eicosyl chloroformate (prepared by reacting 1-eicosanol with phosgene) is slowly added to the reaction system at a temperature from 20°-25°C. The reaction system is stirred at this temperature for 3 hours at which time the reaction solution is added to 250 hydrocarbon thinner which is a mixture of aromatics, paraffins and naphthenes. The organic solution is washed with brine and then stripped to remove volatiles to yield a dispersant product containing eicosyl carbamate functionalities.
  • 1,440 g of eicosyl chloroformate prepared by reacting 1-eicosanol with phosgene
  • the reaction solution is added to 250 hydrocarbon thinner which is a mixture of aromatics, paraffins and naphthenes.
  • the organic solution is washed with brine and then stripped to remove volatile
  • TLC thin layer chromatography
  • a sample of mono-trichloroacetate was purified by silica gel chromatography.
  • the crude material (90.8 g) was placed on a column packed with 484 g of silica gel and eluted with 5% ethyl acetate/hexane.
  • IR shows hydroxy at 3400 cm -1 and carbonyl at 1765 cm -1 .
  • NMR (CDC I3 ) shows ⁇ H(-OH) at delta 3.35, 2H(-CH 2 -O) at delta 4.0 and 2H(C-O-CH 2 -C) at delta 4.55.
  • Ethylene glycol mono-trichloroacetate 14.5 g, 0.07 moles, was dissolved in 100 ml of toluene and excess phosgene was carefully passed through the solution for several hours. (The reaction was performed in a well ventilated hood and a KOH scrubber was used to destroy unreacted phosgene and HCl gas). The reaction was monitored by TLC until all of the starting material was gone. After the reaction was completed, nitrogen was bubbled through the solution to remove any unreacted phosgene. The toluene solution containing the chloroformate can be used in subsequent reactions.
  • the trichloroacetyl group may be removed as follows: A 5 ml sample from (a) above was added to 10 ml of hexane and about 0.25 ml of di-n-butyl amine. Afterwards, the solution was stirred in a 50 ml flask at room temperature overnight and then heated to 40°C for 40 minutes, followed by 2 additional hours at room temperature. An aliquot was then removed and stripped. Infrared analysis of this sample indicated that the trichloroacetyl group had been removed. The reaction mixture was then washed several times with brine and then stripped under vacuum to yield a product identical to that produced in (b) above.
  • Example 46 (a) The chloroformate of ethylene glycol mono-trichloroacetate, 1.7 g, was dissolved in 25 ml toluene. 3.8 g of a bissuccinimide (prepared by reacting 1 mole of dodecenyl succinic anhydride with 0.5 mole of diethylene triamine to yield the bissuccinimide) was dissolved in 35 ml of toluene. Both solutions were cooled to below 0°C (approximately -2°C) using a salt ice-water bath. The solutions were poured together into a flask equipped with a mechanical stirrer and drying tube.
  • a bissuccinimide prepared by reacting 1 mole of dodecenyl succinic anhydride with 0.5 mole of diethylene triamine to yield the bissuccinimide
  • reaction solution was mixed with strong stirring and kept below 0°C for 40 minutes and then allowed to warm to room temperature. After reaction completion, the reaction solution was stripped under vacuum to yield a crude product.
  • This product was purified by column chromatography using 80 g silica gel and 1:1 ethyl acetate/hexane as the eluting solvent to recover 3.7 g of the trichloroacetyl ethyl carbamate of the bissuccinimide. Infrared analysis shows a trichloroacetyl band at 1770 cm -1 and succinimide and carbamate bands at 1710-1690 cm -1 .
  • Glycerol di-(trichloroacetate) 36.1 g is dissolved in 200 ml of toluene and excess phosgene is carefully passed through the solution for several hours. (The reaction is preformed in a well ventilated hood and a KOH scrubber is used to destroy unreacted phosgene and HCl gas.) The reaction is monitored by TLC until all of the starting material is gone. After reaction completion, nitrogen is bubbled through the solution to remove any unreacted phosgene to yield a toluene solution containing the title product.
  • Example 49 The chloroformate of glycerol di ( trichloroacetate), 42.3 g, is dissolved in 200 ml toluene.
  • 300 g of a monosuccinimide dispersant composition (prepared by reacting 1 mole of polyisobutenyl succinic anhydride, where the polyisobutenyl group has a number average molecular weight of about 950, with 0.87 mole of tetraethylene pentaamine then diluting to about 50% actives in diluent oil) is dissolved in 200 ml toluene. Both solutions are cooled to below 0°C (approximately -2°C) using a salt ince-water bath.
  • the solutions are poured together into a 2 1 flask equipped with a mechanical stirrer and a drying tube.
  • the reaction solution is mixed with strong stirring and kept below 0°C for 40 minutes and then is allowed to warm to room temperature. After stirring at room temperature for several hours, about 65 mis of the reaction mixture is added to 130 mis hexane and 65 mis IN NaOH in a separatory funnel in order to remove the trichloroacetate group.
  • the mixture is intermittantly shaked for 30 minutes. After phase separation, the organic layer is washed several times with brine, is dried over anhydrous magnesium sulfate, is filtered and stripped to yield dihydroxypropyl carbamate derivatives of the monosuccinimide.
  • the chloroformate of the polyethylene glycol monotrichloroacetate is prepared which then is reacted with a succinimide of this invention and then is then deprotected to yield a succinimide wherein one or more of the basic nitrogens has been converted to a hydroxy polyoxyethylene carbamate.
  • alkylene glycols may be substituted for ethylene glycol: 1,3-propyl-ene glycol; 1,3-butanediol; 1,4-butanediol; 1,4-pentanediol; 1,5-pentanediol; 1,6-hexanediol; 1,9-nonanediol; 1,10-decanediol; 1,2-octadecanediol; 1,2-hexadecanediol; pentaerythritol and glucose.
  • Example 51 To a 500-ml 3-neck flask equipped with a stirrer. Dean-Stark trap, condensor and nitrogen inlet is charged 106 grams (1 equivalent) of a multiply adducted alkenyl succinic anhydride [having a saponification number of 147, prepared from maleic anhydride and polyisobutene of number average molecular weight of 950 and having an average of 1.5 equivalents of succinic groups per alkenyl group]. To the reaction system is added 13.1 grams of tetraethylene pentaamine (0.5 equivalents). The system is heated and stirred at 160°C for 3 hours. The reaction is then stopped and upon cooling to room temperature,
  • Formulated oils containing different modified succinimides of the invention were tested in a Sequence V-D Test method (according to candidate test for ASTM). This procedure utilizes a Ford 2.3-liter, four-cylinder Pinto engine. The test method simulates a type of severe field test service characterized by a combination of low speed, low temperature "stop and go" city driving and moderate turnpike operation. The effectiveness of the additives in the oil is measured in terms of the protection against sludge and varnish deposits on a 0 to 10 scale with 0 being black and 10 indicating no varnish or sludge deposits. The result are indicated in Table II.
  • Example 53 In some cases, succinimides which give superior results in spark-ignition engines give less than desirable performance in diesel engines. However, the modified succinimides of the instant invention give diesel engine dispersancy performance comparable to succinimides as reported below.
  • the compositions of this invention were tested in a Caterpillar 1-G2 test in which a single-cylinder diesel engine having a 5-1/8" (13 cm) bore by 6-1/2" (16.5 cm) stroke is operated under the following conditions: timing, degrees BTDC, 8; brake mean effective pressure, psi 141 (9,913 gms/cm 2 ); brake horsepower 42 (448,837.2 Cal., gm/min); Btu's per minute 5850 (88,456 Cal., kg/min); speed 1800 RPM; air boost, 53" (134.6 cm) Hg absolute, air temperature in, 255°F (123.9°C); water temperature out, 190°F (87.8°C); and sulfur in fuel, 0.4%.
  • the base oil used in these tests is a mid-Continent base stock SAE 30 oil containing 18 mmols/kg of a zinc dihydrocarbyl dithiophosphate, 36 mmols/kg of an overbased calcium phenate, and the amount noted in the table of dispersant.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Lubricants (AREA)
  • Pyrrole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP87905836A 1986-08-15 1987-08-13 Modifizierte succinimide Expired - Lifetime EP0277222B1 (de)

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US897190 1986-08-15
US06/897,190 US4747965A (en) 1985-04-12 1986-08-15 Modified succinimides

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EP (1) EP0277222B1 (de)
CA (1) CA1324385C (de)
DE (2) DE277222T1 (de)
WO (1) WO1988001290A1 (de)

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DE3784157T2 (de) 1993-09-23
EP0277222A1 (de) 1988-08-10
WO1988001290A1 (en) 1988-02-25
EP0277222B1 (de) 1993-02-10
DE277222T1 (de) 1989-03-30
DE3784157D1 (de) 1993-03-25
US4747965A (en) 1988-05-31
CA1324385C (en) 1993-11-16

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